Carboplatin Dosing in Children: Calculation by Different Formulae

被引:0
|
作者
Wuerthwein, Gudrun [2 ]
Krefeld, Barbara [1 ]
Gerss, Joachim [3 ]
Boos, Joachim [1 ]
机构
[1] Univ Klinikum Munster, Klin & Poliklin Kinderheilkunde Padiatr Hamatol O, D-48129 Munster, Germany
[2] ZKS, Freiburg, Germany
[3] Univ Klinikum Munster, Abt Med Informat & Biomath, Munster, Germany
来源
ONKOLOGIE | 2011年 / 34卷 / 1-2期
关键词
Carboplatin; Dose calculation; Children; GLOMERULAR-FILTRATION-RATE; BODY-SURFACE AREA; SERUM CREATININE; POPULATION PHARMACOKINETICS; PLASMA CREATININE; RENAL-FUNCTION; SOLID TUMORS; PHASE-I; WEIGHT; HEIGHT;
D O I
10.1159/000323369
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Carboplatin dosing in children is based on renal function and there exists a wealth of formulae available for calculating the body surface area (BSA), the glomerular filtration rate (GFR), and the carboplatin dose. Patients and Methods: A fictitious group of children with different ages and body builds was 'constructed'. For comparison of formulae, bias and precision were assessed. Results: BSA calculations according to DuBois-DuBois, Gehan-George, Mosteller, and Boyd showed good agreement. GFR calculations according to the weight-based Cole formula and the Leger formula gave comparable results. Regarding GFR in young children, the weight- and creatinine-based Cole and the Schwartz formula showed clear differences. Again, carboplatin dose calculations according to Marina, Newell, and Chatelut are comparable. Moreover, the precision of the creatinine measurement has a clear influence on the result of the dose calculation. Conclusions: The choice of the GFR formula is more important for the carboplatin dose calculation compared to the BSA or dose equation. GFR calculations in children show marked, age-dependent variations. A sequence of multiple calculation steps (especially for the Schwartz and Marina formulae) may lead to considerable uncertainty and proneness to error in the clinical routine. In high-risk patients, GFR should be measured precisely and complemented by therapeutic drug monitoring.
引用
收藏
页码:16 / 22
页数:7
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